Variant (rsID / SNP)

rs10770865

rs10770865 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC9. Location: chromosome 12, position 22,063,115. Clinical significance in the table: Benign.

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Reference-table entries

ABCC9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:22063115
Cytoband: 12p12.1
HGVS: NM_020297.4(ABCC9):c.1296= (p.Pro432=)
Allele change: Synonymous_P432P

Associated conditions / phenotypes

Cardiovascular phenotype|Dilated cardiomyopathy 1O|Hypertrichotic osteochondrodysplasia Cantu type|Cardiomyopathy

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.